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Neurology|June 25, 2010
Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiencyS A Mullen, A Suls, P De Jonghe, et al.
Neurology|May 21, 2010
Four generations of epilepsy caused by an inherited microdeletion of the SCN1A geneA Suls, R Velizarova, I Yordanova, et al.
Neurology|August 23, 2006
A novel GABRG2 mutation associated with febrile seizuresD Audenaert, E Schwartz, K G Claeys, et al.
Neurology|April 27, 2007
Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9qL Deprez, K Peeters, W Van Paesschen, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Neurology|July 15, 2011
De novo SCN1A mutations in migrating partial seizures of infancyD Carranza Rojo, L Hamiwka, J M McMahon, et al.
Neurology|December 2, 2011
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiencyV Guergueltcheva, K Peeters, J Baets, et al.
Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
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